2018
DOI: 10.37358/mp.18.4.5080
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Operational Procedures in the Theory of the Drug Release from Chitosan Hydrogels

Abstract: We build a theoretical model based on a generalization of harmonic applications of Misner-type. It results a sine-Gordon type fractal differential equation whose elliptical solutions can describe, through a convenient choice of fractal dynamic constants, various modes of drug release. Thus, the entire class of empirical models (Higuchi, Korsmeyer-Peppas, Peppas-Sahlin) describing the drug release processes can be dispensed with.

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Cited by 2 publications
(2 citation statements)
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References 13 publications
(21 reference statements)
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“…Pellets of drug delivery samples with a mass of 62 mg were immersed in a volume of 10 mL PBS and kept at 37 °C. At certain times, 2 mL of supernatant was removed from the vials and replaced with PBS, maintaining a constant volume of 10 mL [ 23 , 24 ]. The concentration of the drug in the supernatant was determined by UV-Vis spectroscopy, according to Lambert–Beer law, using the maximum of absorbance from 275 nm, and fitting the value on a previously drawn calibration curve.…”
Section: Methodsmentioning
confidence: 99%
“…Pellets of drug delivery samples with a mass of 62 mg were immersed in a volume of 10 mL PBS and kept at 37 °C. At certain times, 2 mL of supernatant was removed from the vials and replaced with PBS, maintaining a constant volume of 10 mL [ 23 , 24 ]. The concentration of the drug in the supernatant was determined by UV-Vis spectroscopy, according to Lambert–Beer law, using the maximum of absorbance from 275 nm, and fitting the value on a previously drawn calibration curve.…”
Section: Methodsmentioning
confidence: 99%
“…Moreover, the innate thixotropy of the gels permits their targeted injection and sets the bases for a prolonged local release at the injection site (in this case, the peritoneal cavity), which assures the much-desired combination of maximum local effect and minimum overall side effects. The drug release behavior, as followed by UV–Vis and various theoretical mathematic models, consists of a prolonged, diffusion-controlled mechanism starting from the outer layers of the hydrogels [ 101 ]. The system with the lowest citral concentration acted as the best drug reservoir, releasing roughly 65% of the anticancer reagent in 32 h. The chitosan-based matrices showed in vivo side effects that were comparable and most likely belonging to the pure drug and a lysozyme-triggered enzymatic degradation (11% mass loss after 21 days).…”
Section: Glycodynameric Gels For Drug Deliverymentioning
confidence: 99%